Canonical Allele Identifier: CA1926639403

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014376A= , CM000672.2:g.89014376A=	GRCh38
NC_000010.10:g.90774133A= , CM000672.1:g.90774133A=	GRCh37
NC_000010.9:g.90764113A=	NCBI36
NG_009089.2:g.28846A= , LRG_134:g.28846A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1243A=
ENST00000355740.8:c.*257A=	ENSP00000347979.3:n.*257A=
ENST00000357339.7:c.871A=	ENSP00000349896.2:p.Thr291=
ENST00000371857.8:n.2479A=
ENST00000460510.6:c.217A=	ENSP00000512812.1:p.Thr73=
ENST00000466081.6:n.2583A=
ENST00000477270.6:c.979A=	ENSP00000512813.1:p.Thr327=
ENST00000479522.6:c.*363A=	ENSP00000424113.1:n.*363A=
ENST00000484444.6:c.*375A=	ENSP00000420975.1:n.*375A=
ENST00000488877.6:c.825A=	ENSP00000425159.1:n.825A=
ENST00000492756.7:c.*363A=	ENSP00000422453.1:n.*363A=
ENST00000494799.6:c.217A=	ENSP00000512834.1:p.Thr73=
ENST00000562983.3:c.217A=	ENSP00000512845.1:p.Thr73=
ENST00000612663.6:c.*336A=	ENSP00000477997.3:n.*336A=
ENST00000640140.2:n.1079A=
ENST00000640250.2:n.433A=
ENST00000640681.2:n.1038A=
ENST00000696723.1:n.4567A=
ENST00000696741.1:n.2572A=
ENST00000696742.1:n.2299A=
ENST00000696743.1:n.3702A=
ENST00000696744.1:n.973A=
ENST00000696767.1:n.1268A=
ENST00000696768.1:c.*257A=	ENSP00000512859.1:n.*257A=
ENST00000696769.1:n.2623A=
ENST00000696771.1:c.217A=	ENSP00000512860.1:p.Thr73=
ENST00000696772.1:n.2537A=
ENST00000696773.1:n.2276A=
ENST00000696774.1:n.6044A=
ENST00000696776.1:c.1027A=	ENSP00000512861.1:p.Thr343=
ENST00000696777.1:n.2342A=
ENST00000696778.1:n.1370A=
ENST00000696779.1:c.541A=	ENSP00000512862.1:p.Thr181=
ENST00000696780.1:c.964A=	ENSP00000512863.1:p.Thr322=
ENST00000696781.1:c.679A=	ENSP00000512864.1:p.Thr227=
ENST00000696782.1:c.*336A=	ENSP00000512865.1:n.*336A=
ENST00000696783.1:n.2802A=
ENST00000696992.1:n.2051A=
ENST00000696995.1:n.4463A=
ENST00000696996.1:n.2376A=
ENST00000696997.1:c.*564A=	ENSP00000513028.1:n.*564A=
ENST00000696998.1:n.2188A=
ENST00000696999.1:c.217A=	ENSP00000513029.1:p.Thr73=
ENST00000697036.1:c.*350A=	ENSP00000513060.1:n.*350A=
ENST00000697037.1:n.969A=
ENST00000697093.1:n.3170A=
ENST00000697094.1:n.3517A=
ENST00000697095.1:c.*2135A=	ENSP00000513104.1:n.*2135A=
ENST00000697096.1:n.2067A=
ENST00000697097.1:c.217A=	ENSP00000513105.1:p.Thr73=
ENST00000562983.2:n.1120A=
ENST00000690268.1:c.1015A=	ENSP00000509810.1:p.Thr339=
ENST00000355740.7:c.*260A=	ENSP00000347979.3:n.*260A=
ENST00000612663.5:c.*336A=	ENSP00000477997.3:n.*336A=
ENST00000640140.1:n.1106A=
ENST00000640250.1:n.433A=
ENST00000640681.1:n.1055A=
ENST00000652046.1:c.934A= MANE Select	ENSP00000498466.1:p.Thr312=
ENST00000352159.8:c.*251A=	ENSP00000345601.4:n.*251A=
ENST00000355279.2:c.909A=	ENSP00000347426.2:n.909A=
ENST00000355740.6:c.934A=	ENSP00000347979.2:p.Thr312=
ENST00000357339.6:c.871A=	ENSP00000349896.2:p.Thr291=
ENST00000479522.5:c.*363A=	ENSP00000424113.1:n.*363A=
ENST00000484444.5:c.*375A=	ENSP00000420975.1:n.*375A=
ENST00000488877.5:c.*375A=	ENSP00000425159.1:n.*375A=
ENST00000492756.5:c.762A=	ENSP00000422453.1:n.762A=
ENST00000494410.5:c.*292A=	ENSP00000423755.1:n.*292A=
ENST00000612663.4:c.*281A=	ENSP00000477997.2:n.*281A=
NM_000043.4:c.934A= , LRG_134t1:c.934A=	NP_000034.1:p.Thr312=
NM_152871.2:c.871A=	NP_690610.1:p.Thr291=
NM_152872.2:c.*246A=	NP_690611.1:n.*246A=
NR_028033.2:n.1108A=
NR_028034.2:n.970A=
NR_028035.2:n.1033A=
NR_028036.2:n.1171A=
XM_006717819.2:c.1015A=	XP_006717882.1:p.Thr339=
XM_011539764.1:c.1096A=	XP_011538066.1:p.Thr366=
XM_011539765.1:c.1033A=	XP_011538067.1:p.Thr345=
XM_011539766.1:c.1015A=	XP_011538068.1:p.Thr339=
XM_011539767.1:c.979A=	XP_011538069.1:p.Thr327=
XR_945733.1:n.939A=
NM_000043.5:c.934A=	NP_000034.1:p.Thr312=
NM_001320619.1:c.*257A=	NP_001307548.1:n.*257A=
NM_152871.3:c.871A=	NP_690610.1:p.Thr291=
NM_152872.3:c.*246A=	NP_690611.1:n.*246A=
NR_028033.3:n.1080A=
NR_028034.3:n.942A=
NR_028035.3:n.1005A=
NR_028036.3:n.1143A=
NR_135313.1:n.1060A=
NR_135314.1:n.1243A=
NR_135315.1:n.996A=
XM_006717819.3:c.1015A=	XP_006717882.1:p.Thr339=
XM_011539764.2:c.1096A=	XP_011538066.1:p.Thr366=
XM_011539765.2:c.1033A=	XP_011538067.1:p.Thr345=
XM_011539766.2:c.1015A=	XP_011538068.1:p.Thr339=
XM_011539767.3:c.979A=	XP_011538069.1:p.Thr327=
XR_945732.3:n.1002A=
XR_945733.2:n.939A=
NM_000043.6:c.934A= MANE Select	NP_000034.1:p.Thr312=
NM_001320619.2:c.*257A=	NP_001307548.1:n.*257A=
NM_152871.4:c.871A=	NP_690610.1:p.Thr291=
NM_152872.4:c.*246A=	NP_690611.1:n.*246A=
NR_028033.4:n.841A=
NR_028034.4:n.703A=
NR_028035.4:n.766A=
NR_028036.4:n.904A=
NR_135313.2:n.821A=
NR_135314.2:n.1100A=
NR_135315.2:n.853A=